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Senior Machinist
Requirements:
Job Scope:
Lee Wan Ling | Reg No: R23116154
THE SUPREME HR ADVISORY PTE LTD | EA No: 14C7279
Official account of Jobstore.
Reporting to the Assistant Director, Enterprise Information Security Engineering (EIS), this Sr. Staff Information Security Engineer plays an important tactical role at Illumina. Member of an enterprise-wide and global Information Security team, this position participates in the deployment and support of controls and processes that protect the company’s data. This key role interacts globally across all business units, performs technical reviews, technical security control testing, gap analysis, risk evaluation, and provides subject-matter expertise for solutions deployed and supported by the Information Security department. Support of program controls and processes to ensure mitigation of risks and approved configuration certification of the entire Illumina environment. This position requires extensive knowledge, experience, and proven skills in the areas of engineering, architecture, and design, especially within the SCADA, Operational Technology (OT) and Internet of Things (IoT) space.
Support includes understanding and enforcing of established processes, analysis of cloud and on-premises computing environment, coordination of project responsibilities, testing, documentation, technical diagraming, cybersecurity-based awareness and education, and participation in periodic audits. Performs all duties in accordance with the company’s policies and procedures, all state, federal, and country laws and regulations, wherein the company operates. Delivery of activity reporting, including metrics, environment impact, effectiveness progress, and performance indicators. The role will also assist with ensuring discretionary and regulatory audits are aligned with Illumina’s current processes and procedures.
Duties & Responsibilities
Qualifications
Education
#LI-HYBRID
#illuminacareers
Official account of Jobstore.
Responsibilities
Requirements
Please kindly email your resume in Ms Word to hr@xtalents.com.sg
We regret to inform that only shortlisted candidates would be notified.
Registration Number: R1328870
EA License No. 22C1026
Official account of Jobstore.
Reporting to the Assistant Director, Enterprise Information Security Engineering (EIS), this Sr. Staff Information Security Engineer plays an important tactical role at Illumina. Member of an enterprise-wide and global Information Security team, this position participates in the deployment and support of controls and processes that protect the company’s data. This key role interacts globally across all business units, performs technical reviews, technical security control testing, gap analysis, risk evaluation, and provides subject-matter expertise for solutions deployed and supported by the Information Security department. Support of program controls and processes to ensure mitigation of risks and approved configuration certification of the entire Illumina environment. This position requires extensive knowledge, experience, and proven skills in the areas of engineering, architecture, and design, especially within the SCADA, Operational Technology (OT) and Internet of Things (IoT) space.
Support includes understanding and enforcing of established processes, analysis of cloud and on-premises computing environment, coordination of project responsibilities, testing, documentation, technical diagraming, cybersecurity-based awareness and education, and participation in periodic audits. Performs all duties in accordance with the company’s policies and procedures, all state, federal, and country laws and regulations, wherein the company operates. Delivery of activity reporting, including metrics, environment impact, effectiveness progress, and performance indicators. The role will also assist with ensuring discretionary and regulatory audits are aligned with Illumina’s current processes and procedures.
Duties & Responsibilities
Qualifications
Education
#LI-HYBRID
#illuminacareers
Official account of Jobstore.
Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you'll help bring medicines to the world even faster by imagining what’s possible and taking action.
Working with Pfizer’s dynamic engineering team, you will play a critical role in the management of manufacturing information systems to improve manufacturing success rates and ensuring zero down time.
As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams.
It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe.
Contribute to the completion of projects, manage own time on agreed targets, develop plans for own projects and leads small project teams.
Monitor, generate and complete the periodic review, validation master plan for the automation engineering program.
Demonstrate good planning, organizing, time management and team participation skills.
Responsible for routine and preventive maintenance work, ensure all the equipment and facilities work safely, efficiently and reliably.
Generate and develop standard operating procedures and system support.
Analyze operational process problems and recommend appropriate corrective and preventative actions.
Manage change control authoring and execution.
Participate in the site and network wide teams to provide cybersecurity alignment and direction.
Provide 24x7x365 support of our automation systems and perform automation activities for capital and non-capital projects.
Modify moderately complex to highly complex control logic that requires a degree of scientific and/or manufacturing process expertise.
Mentor and guide junior staff and serve as a technical trainer, whenever necessary.
Clearly communicate progress and issues to peers, customers, and project managers.
Applicant must have a High School Diploma (or Equivalent) and 8 years of relevant experience.
OR an Associate's degree with 6 years of experience.
OR a Bachelor's with at least 3 years of experience.
OR Master's with more than 1 year of experience.
3+ years of demonstrated experience in Automation Engineering.
Experience with writing software test plans, user requirements, and system design documents.
Experience on Automation Compliance projects.
Familiar with process controls equipment.
Strong knowledge of Computerized Systems, Compliance regulations and standards.
Understanding of programming, and proficiency in at least one language.
Teamwork spirit, good communication skills and training abilities.
Ability to learn new technologies and adapt to change.
Relevant pharmaceutical manufacturing experience
PHYSICAL/MENTAL REQUIREMENTS
light lifting, sitting, standing, walking, bending.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Travel less than 10% (typically training or equipment acceptance testing)
Work Location Assignment: On Premise
Other Job Details:
Last Date to Apply for Job: March 31, 2024
Eligible for Relocation Package
Eligible for Employee Referral Bonus
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Official account of Jobstore.
The Role:
Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.
Moderna is solidifying its footprint in Basel, the vibrant hub of pharmaceutical innovation in Switzerland, to further our mission of delivering the greatest possible impact to people through mRNA medicines. As we grow our international operations and commercial activities in Basel, we invite global talents to join us in this exciting journey of transforming medicine and impacting lives worldwide.
Moderna is seeking a dedicated and innovative Senior Engineer I to join our Manufacturing Science and Technology (MS&T) department. This pivotal role is designed for a passionate individual who will be instrumental in supporting our Contract Manufacturing Organization (CMO) activities, primarily focusing on lipid nanoparticle manufacturing in Granada, Spain. As a key player in the external MS&T team, you will also extend your expertise to support plasmid and custom-made small molecule production at CMOs. The successful candidate will forge strong collaborative ties with CMOs and internal teams—including External Manufacturing, Supply Chain, Regulatory, and Quality—to ensure flawless execution of technology transfer and ongoing technical support. Your contributions will be critical in upholding Moderna's commitment to innovation and excellence in the biotechnology field.
Here’s What You’ll Do:
Your key responsibilities will be:
Support technology transfer activities for commercial products into CMOs, ensuring seamless integration and operational excellence.
Provide robust technical support for cGMP manufacturing processes at CMOs, including authoring technology transfer documents, addressing change controls, and assisting with manufacturing investigations, deviations, and leading process validation activities.
Conduct thorough data reviews and analyses to evaluate manufacturing performance, authoring comprehensive summary reports.
Lead cross-functional teams in troubleshooting, identifying, and implementing operational improvements for manufacturing processes and equipment.
Maintain synergy with global manufacturing sites by sharing knowledge, data, and solutions to common manufacturing challenges.
Your responsibilities will also include:
Demonstrating leadership in process development or operational experience in bioprocessing unit operations such as enzymatic reactions, chromatography, nanoparticle manufacturing, and tangential flow filtration.
Familiarity with cGMP environments and single-use equipment is highly advantageous.
Proficiency in English with excellent verbal and written communication skills; knowledge of Spanish is favorable.
The key Moderna Mindsets you’ll need to succeed in the role:
We pursue options in parallel: Your role will demand managing multiple projects and priorities concurrently to ensure the best outcomes in technology transfer and manufacturing support.
We pivot fearlessly: Given the dynamic nature of manufacturing processes and the need for constant innovation, a fearless approach to embracing and leading change is crucial.
Here’s What You’ll Need (Minimum Qualifications):
M.S. or Ph.D. in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Engineering, or a related technical discipline.
A minimum of 5 years of related work experience in the pharmaceutical manufacturing industry.
Demonstrable process development or operational experience in bioprocessing unit operations such as enzymatic reactions, chromatography, nanoparticle manufacturing and tangential flow filtration.
Familiarity with cGMP environments and single-use equipment is highly advantageous.
Proficiency in English with excellent verbal and written communication skills; knowledge of Spanish is favorable.
Proven ability to manage complex projects in a dynamic, fast-paced environment.
Capacity to effectively collaborate in a dynamic, cross-functional matrix environment.
Flexibility and adaptability to meet the challenges of new and evolving technical opportunities in a rapidly changing environment.
Here’s What You’ll Bring to the Table (Preferred Qualifications)
Demonstrated ability to drive projects to completion with minimal supervision.
Proven track record of problem-solving and innovation in bioprocessing operations.
Strong analytical skills with the ability to make data-driven decisions.
Experience in a multinational organization with the ability to navigate cultural and operational complexities.
A proactive, forward-thinking approach that anticipates and addresses challenges before they arise.
Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.
We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)
-
Official account of Jobstore.
The Role:
Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.
At the heart of Spain's Andalusia region, Moderna is solidifying its global presence by collaborating closely with a local CMO in Granada. This strategic partnership leverages Granada's rich history in science and innovation, focusing on the active substance manufacturing critical to our mRNA medicines. Our Granada team plays a pivotal role in our supply chain, ensuring the seamless production and global distribution of our transformative healthcare solutions. We are seeking dedicated professionals who are passionate about leveraging cutting-edge biotechnology to make a substantial impact on global health. Join us in Granada, where tradition meets innovation, to contribute to our mission of pioneering mRNA technology and improving lives worldwide.
Moderna is seeking a dedicated and innovative Senior Engineer I to join our Manufacturing Science and Technology (MS&T) department. This pivotal role is designed for a passionate individual who will be instrumental in supporting our Contract Manufacturing Organization (CMO) activities, primarily focusing on lipid nanoparticle manufacturing in Granada, Spain. As a key player in the external MS&T team, you will also extend your expertise to support plasmid and custom-made small molecule production at CMOs. The successful candidate will forge strong collaborative ties with CMOs and internal teams—including External Manufacturing, Supply Chain, Regulatory, and Quality—to ensure flawless execution of technology transfer and ongoing technical support. Your contributions will be critical in upholding Moderna's commitment to innovation and excellence in the biotechnology field.
Here’s What You’ll Do:
Your key responsibilities will be:
Support technology transfer activities for commercial products into CMOs, ensuring seamless integration and operational excellence.
Provide robust technical support for cGMP manufacturing processes at CMOs, including authoring technology transfer documents, addressing change controls, and assisting with manufacturing investigations, deviations, and leading process validation activities.
Conduct thorough data reviews and analyses to evaluate manufacturing performance, authoring comprehensive summary reports.
Lead cross-functional teams in troubleshooting, identifying, and implementing operational improvements for manufacturing processes and equipment.
Maintain synergy with global manufacturing sites by sharing knowledge, data, and solutions to common manufacturing challenges.
Your responsibilities will also include:
Demonstrating leadership in process development or operational experience in bioprocessing unit operations such as enzymatic reactions, chromatography, nanoparticle manufacturing, and tangential flow filtration.
Familiarity with cGMP environments and single-use equipment is highly advantageous.
Proficiency in English with excellent verbal and written communication skills; knowledge of Spanish is favorable.
The key Moderna Mindsets you’ll need to succeed in the role:
We pursue options in parallel: Your role will demand managing multiple projects and priorities concurrently to ensure the best outcomes in technology transfer and manufacturing support.
We pivot fearlessly: Given the dynamic nature of manufacturing processes and the need for constant innovation, a fearless approach to embracing and leading change is crucial.
Here’s What You’ll Need (Minimum Qualifications):
M.S. or Ph.D. in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Engineering, or a related technical discipline.
A minimum of 5 years of related work experience in the pharmaceutical manufacturing industry.
Demonstrable process development or operational experience in bioprocessing unit operations such as enzymatic reactions, chromatography, nanoparticle manufacturing and tangential flow filtration.
Familiarity with cGMP environments and single-use equipment is highly advantageous.
Proficiency in English with excellent verbal and written communication skills; knowledge of Spanish is favorable.
Proven ability to manage complex projects in a dynamic, fast-paced environment.
Capacity to effectively collaborate in a dynamic, cross-functional matrix environment.
Flexibility and adaptability to meet the challenges of new and evolving technical opportunities in a rapidly changing environment.
Here’s What You’ll Bring to the Table (Preferred Qualifications)
Demonstrated ability to drive projects to completion with minimal supervision.
Proven track record of problem-solving and innovation in bioprocessing operations.
Strong analytical skills with the ability to make data-driven decisions.
Experience in a multinational organization with the ability to navigate cultural and operational complexities.
A proactive, forward-thinking approach that anticipates and addresses challenges before they arise.
Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.
We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)
-
Official account of Jobstore.
Responsibilities
Requirements
Please kindly email your resume in Ms Word to hr@xtalents.com.sg
We regret to inform that only shortlisted candidates would be notified.
Registration Number: R1328870
EA License No. 22C1026
Official account of Jobstore.
Responsibilities
Requirements
Please kindly email your resume in Ms Word to hr@xtalents.com.sg
We regret to inform that only shortlisted candidates would be notified.
Registration Number: R1328870
EA License No. 22C1026
Official account of Jobstore.
About Pierce, an Oshkosh company
At Pierce Manufacturing, we build trucks that protect people and communities around the world. To our team, there is no room for anything less than providing the absolute best. Since 1913, building truck bodies on Model T Ford chassis in an old converted church has evolved to creating highly customized, carefully designed and engineering pumpers, aerials, tankers and rescue units that have no equal. Today, you'll find more than 30,000 Pierce apparatuses on the road that are making a difference in people's lives, every day. To us, every step in the process of building our trucks is personal. From innovation and expertise, to the customization and service. Our trucks are designed to perform under the toughest conditions.
Senior Engineer - Electrical R25936
The Sr Engineer – Electrical designs functional, reliable and cost-effective heavy-duty vehicle high voltage electrical systems. Performs engineering analysis and electrical design or re-design, and development of electrical systems and subsystems into existing and new vehicles. Provides integration and execution support for vehicle control and embedded systems development.
YOUR IMPACT:
MINIMUM QUALIFICATIONS:
STANDOUT QUALIFICATIONS:
CORE COMPETENCIES:
WORKING CONDITIONS:
WHY PIERCE?
Moving the future forward is our priority and this includes your future. We encourage professional development and champion our employees’ success through various skills and training opportunities. Named one of the World’s Most Ethical Companies™ by Ethisphere Institute for six consecutive years, everything we do at Oshkosh is guided by our core values and the 15k+ team members around the world who embody them.
We put people first. We do the right thing. We persevere. We are better together.
We offer our employees an outstanding range of benefits, including:
Visit our Glassdoor Profile
Keep up with us on LinkedIn
*OSH1917
#LI-BB1
Oshkosh is committed to working with and offering reasonable accommodations to job applicants with disabilities. If you need assistance or an accommodation due to a disability for any part of the recruitment process, please contact our reception desk by phone at +1 (920) 502.3009 or our talent acquisition team by email corporatetalentacquisition@oshkoshcorp.com.
Oshkosh Corporation is an Equal Opportunity and Affirmative Action Employer. This company will provide equal opportunity to all individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Information collected regarding categories as provided by law will in no way affect the decision regarding an employment application.
Oshkosh Corporation will not discharge or in any manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with Oshkosh Corporation's legal duty to furnish information.
Certain positions with Oshkosh Corporation require access to controlled goods and technologies subject to the International Traffic in Arms Regulations or the Export Administration Regulations. Applicants for these positions may need to be "U.S. Persons," as defined in these regulations. Generally, a "U.S. Person" is a U.S. citizen, lawful permanent resident, or an individual who has been admitted as a refugee or granted asylum.
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At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon.
As a Spare Parts Executive/ Engineer, you will be tasked to oversee inventory control under our Engineering Department. You will work closely with various Engineering and production team to ensure smooth day to day operations for manufacturing plant.
In this role, a typical day will include:
WHAT YOU’LL BRING TO ALCON:
HOW YOU CAN THRIVE AT ALCON:
Alcon Careers
See your impact at alcon.com/careers
Official account of Jobstore.
SSMC (Systems on Silicon Manufacturing Company Pte. Ltd.), is a Joint Venture between NXP and TSMC. We offer flexible and cost effective semiconductor fabrication solutions by maintaining fully equipped SMIF cleanroom environment, 100% equipment automation and proven wafer-manufacturing processes.
At SSMC, every career journey is unique and rewarding. We're looking for innovative, passionate, and talented people like you to join our team.
We’re searching for a Senior Engineer to be part of our IT Department diverse team of talent. You will be responsible to Engineering Analytic Systems Software development, Design and Support.
What you will be working on:
More About You:
SSMC is committed to equal employment opportunities and abides by the Tripartite Guidelines on Fair Employment Practices (TGFEP). All qualified applicants will receive non-discriminatory consideration for employment on the basis of merit and regardless of age, race, gender, religion, marital status and family responsibilities, or disability, or any other attributes as protected by the relevant laws.
Official account of Jobstore.
Entry level Nitec / Diploma in Engineering X 5 Opening
Junior/Senior / No experience / Entry level welcome apply ( X5 Permanent Role Opening ) URGENT !!!
Good Pay + Good allowance + Good Bonus
Full training provided for Entry Level
The Job
Requirement
Good Pay + Good allowance + Good Bonus
Interested candidates please send an updated Resume / CV in Ms Word format to lilian@recruitflash.com or WhatsApp’s your resume to 98332779 ( no Calls)
Consultant in-charge : Quah Li Lian (Lilian) ( Registration No: R1983286 )
Official account of Jobstore.
Tätigkeitsbeschreibung
Sich etwas Neues trauen, über sich hinauswachsen und dabei die Grenzen des Machbaren neu definieren. Das ist das, was wir bei ZEISS leben.
ZEISS SMT entwickelt und produziert als Technologieführer die weltweit modernsten optischen Systeme für Schlüsselprozesse der Halbleiterindustrie. Dank unserer Technologien werden Chips immer kleiner, leistungsfähiger, energieeffizienter und preiswerter. Damit liefern wir einen wesentlichen Beitrag zur Digitalisierung, die heute schon die ganze Welt verändert.
Als zentrale IT der SMT treiben wir die digitale Transformation des Unternehmens partnerschaftlich mit unseren Fachbereichen in zahlreichen Projekten tagtäglich voran. Der wichtigste Baustein für die erfolgreiche Umsetzung der Roadmap hin zum „Leading Edge“ im Bereich IT und Digital sind großartige Mitarbeiterinnen und Mitarbeiter, die mit voller Überzeugung und Freude am Job die Zukunft des Unternehmens gestalten wollen. Für unseren Bereich IT Application Services suchen wir einen (Senior-) DevOps Engineer (m/w/x) im IT Product Team Manufacturing Services. Neben der Sicherstellung der reibungslosten Applikationsbetriebs unterstützt du aktiv den Softwareentwicklungsprozess und gestaltest damit in konkreten Business-Projekten die Zukunft und Transformation der IT-Landschaft innerhalb unserer Business-Domäne Manufacturing. In diesem technologisch spannenden Umfeld beschäftigst du dich primär mit Kernapplikationen zur Unterstützung der Fertigung der SMT.
Deine Rolle
Als (Senior-) DevOps Engineer übernimmst du die Verantwortung für den Betrieb von (Produktionskritischen-) Softwareapplikationen in einem vom Teamspirit geprägten dynamischen Team von IT-Experten. Dieser basiert auf unseren ITIL-Prozessen (Incident- / Problem- / Configuration- / Change-Management…) und umfasst den gesamten Application-Lifecycle. Die Koordination aller Stakeholder (vom Infrastrukturprovider über die Anwendungsentwickler bis hin zum Kunden) steht im Mittelpunkt deiner Aufgabe. Dies bedarf sowohl sehr guten Kommunikations-Skills als auch einem sehr ausgeprägtem und breiten IT-Betriebswissen (Infrastruktur, Monitoring, Prozesse). Du bist weiterhin integrativer Bestandteil des Softwareentwicklungsteams und bringst deine Erfahrung in Automatisierung, Infrastrukturbereitstellung, Testmanagement und Deployment in den Entwicklungsprozess ein. Dabei bist du aktiver Teilnehmer in diversen Meetings, wie Sprint Planning, Daily/Weekly, Refinement.
Dein Profil
ein erfolgreich abgeschlossenes Studium in Informatik, Wirtschaftsinformatik oder Wirtschaftsingenieurswesen mit Schwerpunkt IT
ca. 3 Jahre Berufserfahrung in einem vergleichbaren Aufgabenumfeld bzw. in einem Produktionsunternehmen mit Fertigung komplexer Produkte
gute Kenntnisse in Microsoft Serverumgebungen, Datenbanken (Oracle, MS-SQL) sowie idealerweise Erfahrung im Bereich Cloudplattformen, vorzugsweise Microsoft Azure
Kenntnisse im Umfeld der Softwareentwicklung samt deren Methoden (Applikationslogging, AzureDevOps, Deployment- und DevOps-Methoden)
Erfahrung in MES-Systemen (wie SAP ME) und SAP ERP sind von Vorteil
idealerweise Kenntnisse in der Überwachung und Automatisierung von Systemen, Abläufen und Prozessen
sehr gute kundenorientierte Kommunikationsfähigkeiten sowie eine strukturierte Arbeitsweise
Your ZEISS Recruiting Team:
Adrian KahlOfficial account of Jobstore.
Responsibilities
Requirements
Please kindly email your resume in Ms Word to hr@xtalents.com.sg
We regret to inform that only shortlisted candidates would be notified.
Registration Number: R1328870
EA License No. 22C1026
Official account of Jobstore.